Product Details

SNP ID
rs146901911
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.11:106009714 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GTTTCTATGTCCTGTGGTTGAAGCA[C/T]GGATTTTTCTCCTTGACCAAGTTCA
Phenotype
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
MSANTD4 PubMed Links

Gene Details

Gene
MSANTD4
Gene Name
Myb/SANT DNA binding domain containing 4 with coiled-coils
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001318747.1 1461 Missense Mutation ATG,GTG M287V NP_001305676.1
NM_001318748.1 1461 Missense Mutation ATG,GTG M287V NP_001305677.1
NM_001318749.1 1461 Missense Mutation ATG,GTG M287V NP_001305678.1
NM_001318750.1 1461 Missense Mutation ATG,GTG M287V NP_001305679.1
NM_032424.2 1461 Missense Mutation ATG,GTG M287V NP_115800.1
XM_011543022.2 1461 Missense Mutation ATG,GTG M287V XP_011541324.1
XM_017018416.1 1461 Missense Mutation ATG,GTG M287V XP_016873905.1
XM_017018417.1 1461 Missense Mutation ATG,GTG M287V XP_016873906.1

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